Clinical Trial Assistant, Hybrid Rotkreuz
- Switzerland
- Clinical Trial Support
- ICON Strategic Solutions
- Remote
About the role
This vacancy has now expired. Please see similar roles below...
As a CTAyou will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Responsibilities include:
• Trial Master File (TMF) creation and management.
• Co-ordinate entry and maintain local data into study management systems including setting up new studies.
• Ensure collection, review, track and provision of appropriate clinical documents to support regulatory submission.
• Track and maintain adequate study related supplies in the office and facilitate their distribution to sites, including preparing and distributing Study File Binders and Site Initiation presentations/materials.
• Process, reconcile, distribute and track essential documents and submit them to local archive in compliance with SOPs.
• Complete tracking documentation as applicable including but not limited to spreadsheets, study and contract tracker.
• Prepare and review site communication documents.
• Set-up/maintain courier accounts and organize shipments.
To be successful in the role, you will have:
• Proficient in speaking and writing German and English
• Previous experience in clinical research
• Excellent organization skills.
• Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business.
• Proficient Microsoft Office applications and use of Internet.
What is offered:
• Unlimited permanent contract
• Friendly work atmosphere
• Compensatory time-off
• Contribution to pension scheme
• Full time
Please feel free to also apply via email to nadine.rabenstein@iconplc.com
Why ICON?
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
Day in the life
Teaser label
Inside ICONContent type
BlogsPublish date
01/26/2023
Summary
The CRO market has seen an unmistakable uplift in demand for its services in recent years. The call for personalised medicine, pricing pressures, and increasing complexity in clinical trials are j
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